Canonical Allele Identifier: CA7657270

Gene: SEMA7A

Linked Data

• ClinVar Variation Id: 3056538
• ClinVar RCV Id: RCV003979185
• dbSNP Id: rs28362914
• ExAC: 15:74710305 G / A
• gnomAD v2: 15-74710305-G-A
• gnomAD v3: 15-74417964-G-A
• gnomAD v4: 15-74417964-G-A
• MyVariant Identifiers: chr15:g.74710305G>A (hg19) ; chr15:g.74417964G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417964G>A , CM000677.2:g.74417964G>A	GRCh38
NC_000015.9:g.74710305G>A , CM000677.1:g.74710305G>A	GRCh37
NC_000015.8:g.72497358G>A	NCBI36
NG_011733.1:g.20995C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.378C>T MANE Select	ENSP00000261918.4:p.Cys126=
ENST00000542748.6:c.-118C>T	ENSP00000441493.1:n.-118C>T
ENST00000261918.8:c.378C>T	ENSP00000261918.4:p.Cys126=
ENST00000542748.5:c.-118C>T	ENSP00000441493.1:n.-118C>T
ENST00000543145.6:c.336C>T	ENSP00000438966.2:p.Cys112=
ENST00000567345.1:c.-118C>T	ENSP00000454365.1:n.-118C>T
NM_001146029.1:c.336C>T	NP_001139501.1:p.Cys112=
NM_001146030.1:c.-118C>T	NP_001139502.1:n.-118C>T
NM_003612.3:c.378C>T	NP_003603.1:p.Cys126=
NM_001146029.2:c.336C>T	NP_001139501.1:p.Cys112=
NM_001146030.2:c.-118C>T	NP_001139502.1:n.-118C>T
NM_003612.4:c.378C>T	NP_003603.1:p.Cys126=
NM_003612.5:c.378C>T MANE Select	NP_003603.1:p.Cys126=
NM_001146029.3:c.336C>T	NP_001139501.1:p.Cys112=
NM_001146030.3:c.-118C>T	NP_001139502.1:n.-118C>T